Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
Application of Array CGH technique for the clinical diagnosis of developmental delay and congenital malformations in Saudi Arabia [400k]
GEO Series GSE182081. Homo sapiens. 52 samples. Type: Genome variation profiling by genome tiling array.
Rare de novo copy number variants in patients with congenital pulmonary atresia
GEO Series GSE56422. Homo sapiens. 21 samples. Type: Genome variation profiling by SNP array.
Severe congenital neutropenia with syndromic features in a patient with homozygous hypomorphic DBF4 mutation
GEO Series GSE160517. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
plasma circRNA-expression profiles in children with pulmonary hypertension secondary to congenital heart disease
GEO Series GSE171827. Homo sapiens. 13 samples. Type: Non-coding RNA profiling by array.
A Switch in Iron Transport Mechanisms Defines Novel Forms of Congenital Chronic Kidney Disease [P15 FeD]
GEO Series GSE100252. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Braf-mutant Schwann cells divert to a repair phenotype to induce congenital demyelinating neuropathy [SCP]
GEO Series GSE262048. Homo sapiens. 29 samples. Type: Expression profiling by high throughput sequencing.
A Novel Acute Erythroleukemia Cell Line Derived from Ascitic Fluid in a Patient with Congenital Acute Myeloid Leukemia
GEO Series GSE264669. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing; Other.
Children with congenital Zika syndrome project - CBQ and GMFCS dataset
<p>Dataset of children with congenital microcephaly due to ZIKV referring to the instruments evaluated CBQ and GMFCS in the year 2021.</p>
Ambulatory Blood Pressure Measurement in Children With Congenital Urine Flow Obstruction
ClinicalTrials.gov study NCT00764543. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Family Study of Congenital Cardiovascular Malformations
ClinicalTrials.gov study NCT00005258. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Tideglusib: Expanded Access Use in Congenital Myotonic Dystrophy
ClinicalTrials.gov study NCT07119775. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Expanded Access Program of TAK-755 for Congenital Thrombotic Thrombocytopenic Purpura (cTTP)
ClinicalTrials.gov study NCT05770219. IPD Sharing: Not stated. Countries: 0. Publications: 0.
TG Gene Mutations and Congenital Hypothyroidism
ClinicalTrials.gov study NCT00493103. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Congenital Esotropia Observational Study (CEOS)
ClinicalTrials.gov study NCT00000163. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Effect of the CTG repeat expansion on RNA splicing in children with congenital myotonic dystrophy
GEO Series GSE126342. Homo sapiens. 42 samples. Type: Expression profiling by high throughput sequencing.
Impaired reorganization of centrosome structure underlies human congenital dilated cardiomyopathy
GEO Series GSE184899. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Tofacitinib reduces skin inflammation in a patient with severe autosomal recessive congenital ichthyosis
GEO Series GSE228449. Homo sapiens. 5 samples. Type: Expression profiling by high throughput sequencing.
The LSD1 inhibitor RN1 rescues Congenital Dyserythropoietic Anemia type II
GEO Series GSE275767. Homo sapiens. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Serial Inversions Induce Tissue-specific Architectural Stripes, Gene Misexpression and Congenital Malformations
GEO Series GSE116794. Mus musculus. 40 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Other; Expression profiling by high throughput sequencing.
Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [ATAC-seq]
GEO Series GSE137330. Mus musculus. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.